PsoriasisPhase 2NCT01988103
Efficacy and Safety Study of Two Doses of Apremilast (CC-10004) In Japanese Patients With Moderate-To-Severe Plaque-Type Psoriasis
A Phase 2 study testing Apremilast in people with Psoriasis and Psoriatic Arthritis, run by Amgen at 56 sites in Japan.
Trial summary
This study will test the clinical effectiveness and safety of two orally administered doses of apremilast compared to placebo in Japanese patients with moderate-to-severe plaque-type psoriasis. Read more about this study
- Who is it for?
- Ages 20 years and older
- Conditions the study is for
- Psoriasis, Psoriatic Arthritis, Psoriasis Arthropatica
- What is being tested?
- Apremilast
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 254 participants
- Where
- 56 sitesJapan
- Study dates
- 9 Jul 2013to 15 Dec 2015
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or female Japanese participants greater than or equal to 20 years of age.
- Diagnosis of chronic, stable plaque psoriasis for at least 6 months prior to screening as defined by: Psoriasis Area Severity Index (PASI) score ≥ 12 and BSA ≥ 10%.
- Psoriasis which is considered inappropriate for topical therapy (based on severity of disease and extent of affected area) or has not been adequately controlled or treated by topical therapy in spite of at least 4 weeks of prior therapy with at least one topical medication for psoriasis or per label.
- In otherwise good health based on medical history, physical examination, 12-lead electrocardiogram (ECG), serum chemistry, hematology, immunology, and urinalysis.
Who cannot join
- Other than psoriasis, history of any clinically significant and uncontrolled systemic diseases; any condition, including the presence of laboratory abnormalities, which would place the participant at unacceptable risk or confound the ability to interpret the data in the study.
- Prior medical history of suicide attempt or major psychiatric illness requiring hospitalization within the last 3 years
- Pregnant or breastfeeding.
- History of or ongoing chronic or recurrent infectious disease.
- Active tuberculosis (TB) or a history of incompletely treated TB.
- Clinically significant abnormality on 12-lead ECG or on chest radiograph at screening.
Show all 15Show fewer
- History of human immunodeficiency virus (HIV) infection or have congenital or acquired immunodeficiencies (eg, Common Variable Immunodeficiency).
- Hepatitis B surface antigen or hepatitis B core antibody positive at screening; positive for antibodies to hepatitis C at screening.
- Malignancy or history of malignancy, except for treated (ie, cured) basal cell or squamous cell in situ skin carcinomas or treated (ie, cured) cervical intraepithelial neoplasia or carcinoma in situ (CIN) of the cervix with no evidence of recurrence within previous 5 years.
- Psoriasis flare within 4 weeks of screening.
- Topical therapy within 2 weeks prior to randomization or systemic therapy for psoriasis or psoriatic arthritis within 4 weeks prior to randomization.
- Use of etretinate within 2 years prior to randomization for females of child bearing potential (FCBP) or within 6 months for males, and within 4 weeks prior to randomization for non-FCBP.
- Use of phototherapy: Ultraviolet light B (UVB), Psoralens and long-wave ultraviolet radiation (PUVA) within 4 weeks prior to randomization or prolonged sun exposure or use of tanning booths or other ultraviolet light sources.
- Use of adalimumab, etanercept, certolizumab pegol, abatacept, tocilizumab, golimumab or infliximab within 12 weeks prior to randomization; use of ustekinumab, alefacept or briakinumab within 24 weeks prior to randomization.
- Any investigational drug within 4 weeks prior to randomization.
Trial locations and contacts
56 sites in 1 country.
56 sites in 1 country
Japan56 sites
Kokubu Medical Office Abashiri Dermatology Clinic
Abashiri-shi, Hokkaido, 093-0016
Chitose Dermatology Plastic Surgery Clinic
Chitose-shi, Hokkaido, 066-0021
Asanuma Dermatology Clinic
Chitose-shi, Hokkaido, 066-0064
Kayaba Dermatology Clinic
Cyu-o-ku, Tokyo, 103-0016
Ekihigashi Hifuka Clinic
Fukuoka, Fukuoka, 812-0013
Tsutsui Clinic Dermatology & Plastic Surgery
Fukuoka, Fukuoka, 813-0042
Yano Hifuka Hinyokika Clini
Fukuoka, Fukuoka, 814-0013
Fukuoka University Hospital
Fukuoka, Fukuoka, 814-0180
HATAMOTO Derma Clinic
Fukuoka, Fukuoka, 815-0075
Tomoko Matsuda Dermatological Clinic
Fukuoka, Fukuoka, 819-0167
Matsuo Clinic
Fukuoka, 719-0373
Tokai University School of Medicine
Hachiōji, Tokyo, 192-0032
Hitachi General Hospital
Hitachi, Ibaraki, 317-0077
TASHIRO Dermatological Clinic
Iizuka-shi, Fukuoka, 820-0040
Inagi Municipal Hospital
Inagi, Tokyo, 206-2801
Tokyo Medical University Ibaraki Medical Center
Inashiki-gun, Ibaraki, 300-0395
TSUTSUMI Clinic
Itabasi-Ku, Tokyo, 174-0071
Okubo Skin Care and Clinic
Itoshima-shi, Fukuoka, 819-1108
Matsuda Dermatology Clinic For Skin, Hair, Nail Diseases
Itoshima-shi, Fukuoka, 819-1116
Kanto Rosai Hospital
Kawasaki, Kanagawa, 211-8510
Teikyo University School of Medicine University Hospital
Kawasaki, Kanagawa, 213-8507
Kawasaki Saiwai Clinic
Kawasaki-shi, Kanagawa, 212-0016
Kitakyushu Municipal Medical Center
Kitakyushu, Fukuoka, 802-0077
Kyushu Kosei Nenkin Hospital
Kitakyushu, Fukuoka, 806-8501
Kyusyu Rosai Hospital
Kitakyushu-shi, Fukuoka, 800-0296
Kokubu Dermatology
Kitami-shi, Hokkaido, 090-0832
Kobe City Medical Center
Kobe, Hyōgo, 653-0013
Koto Hospital
Koto-ku, Tokyo, 136-0072
Maruyama Dermatology Clinic
Koto-ku, Tokyo, 136-0074
Kosumi lin
Kumamoto, Kumamoto, 860-0016
Kumamoto Shinto General Hospital
Kumamoto, Kumamoto, 862-0975
Kurume University Hospital
Kurume, Fukuoka, 830-0011
OIZUMI HANAWA Clinic
Nerima-ku, Tokyo, 178-0063
Matsuo Clinic
Nishiku, Fukuoka, 819-0373
AMC Nishiumeda Clinic
Osaka, 530-0001
Sagamihara National Hospital
Sagamihara, Kanagawa, 252-0392
SANRUI Dermatology
Saitama-shi, Saitama, 330-0854
Kume Derma Clinic
Sakai-Shi, Osaka, 593-8324
Sapporo Skin Clinic
Sapporo, Hokkaido, 060-0063
Fukuzumi Dermatology Clinic
Sapporo, Hokkaido, 062-0042
Kitahara Dermatology Clinic
Setagaya-ku, Tokyo, 158-0094
NAOKO Dermatology Clinic
Setagaya-ku, Tokyo, 158-0097
Mita Dermatology Clinic
Shiba Minato-k, Tokyo, 108-0014
Shakaihoken Simonoseki Kosei Hospital
Shimonoseki-shi, Yamaguchi, 750-0061
Jichi Medical University Hospital
Shimotsuke-shi, Tochigi, 329-0498
NTT Medical Center Tokyo
Shinagawa-ku, Tokyo, 141-8625
Tokyo Medical University Hospital
Shinjyuku-ku, Tokyo, 160-0023
Taneda Dermatology Clinic
Suginami-ku, Tokyo, 166-0015
Federation of National Public Service Personnel Mutual Aid Associations Tachikawa Hospital
Tachikawa, Tokyo, 190-8531
Tokyo Center Clinic
Tokyo, 103-0028
Sugai Dermatologist Park Side Clinic
Utsunomiya, Tochigi, 321-0954
Yame General Hospital
Yame, Fukuoka, 834-0034
Yokohama City University Hospital
Yokohama, Kanagawa, 213-8507
Queen's Square Medical Facilities
Yokohama, Kanagawa, 220-6208
Nomura Dermatology Clinic
Yokohoma City, Kanagawa, 221-0825
Yokosuka Kyosai Hospital
Yokosuka, Kanagawa, 238-8558
About this study
Official title: A Phase 2B, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Two Doses of Apremilast (CC-10004) In Japanese Subjects With Moderate-To-Severe Plaque-Type Psoriasis
This study will test the clinical effectiveness and safety of two orally administered doses of apremilast compared to placebo in Japanese patients with moderate-to-severe plaque-type psoriasis.
Read the detailed description
This is a phase 2b, multicenter, randomized, double-blind, placebo-controlled study of the efficacy and safety of apremilast 20 mg twice a day (BID), apremilast 30 mg BID, and placebo in Japanese participants with moderate to severe plaque psoriasis.
- Conditions
- Psoriasis, Psoriatic Arthritis, Psoriasis Arthropatica
- Being tested
- Apremilast, Placebo
- Keywords
- Psoriasis; Psoriatic Arthritis
- Medical subject headings
- Psoriasis, Arthritis, Psoriatic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ApremilastDrug
Also called CC-10004, Otzela
20 mg tablet BID for 68 weeks
ApremilastDrug
Also called CC-10004, Otzela
20 mg tablet BID for 68 weeks
PlaceboDrug
Placebo tablet BID for 16 weeks
| Study group | Role | What they receive |
|---|---|---|
| Apremilast 20mg | Experimental | Apremilast 20 mg tablets orally twice a day (BID) Receives: Drug: Apremilast; Drug: Placebo |
| Apremilast 30mg | Experimental | Apremilast 30 mg tablets orally BID Receives: Drug: Apremilast; Drug: Placebo |
| Placebo | Placebo comparator | Identically-appearing placebo tablets BID for 16 weeks followed by participants being re-randomized in a blinded fasion to apremilast 20 mg or 30mg tablets BID for 52 weeks Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants Who Achieved a 75% Improvement (Response) From Baseline in the Psoriasis Area and Severity Index (PASI-75) at Week 16
PASI-75 response is the percentage of participants who achieved at least a 75% reduction (improvement) from baseline in PASI score at Week 16. The improvement in PASI score was used as a measure of efficacy. The PASI was a measure of psoriatic disease severity taking into account qualitative lesion characteristics (erythema, thickness and scaling) and degree of skin surface area involvement on defined anatomical regions. PASI scores range from 0 to 72, with higher scores reflecting greater disease severity. Erythema, thickness, and scaling are scored on a scale of 0 (none) to 4 (very severe) on 4 anatomic regions of the body: head, trunk, upper limbs, and lower limbs. Degree of involvement on each of the 4 anatomic regions is scored on a scale of 0 (no involvement) to 6 (90% to 100% involvement). The PASI score was set to missing if any severity score or degree of involvement was missing.
Measured: Baseline to Week 16
Secondary outcomes (12)
Percentage of Participants Who Achieved a Static Physician's Global Assessment (sPGA) Score of Clear (0) or Almost Clear (1) With at Least 2 Point Reduction From Baseline to Week 16
The sPGA is a measure of psoriasis disease severity at the time of evaluation by the Investigator. It does not compare assessments across visits or rely on investigator recall or prior disease. The sPGA is a 6-point scale ranging from 0 (clear, except for residual discoloration) to 5 (severe; majority of plaques have severe thickness, erythema, and scaling). The investigator examines all of the lesions on the participant and assigns a score ranging from 0 to 5 for thickness, erythema and degree of scaling. Scores for thickness, erythema and scaling are then summed and the mean of these 3 scores equals the overall sPGA score.
Measured: Baseline to Week 16
Percent Change From Baseline in the Psoriasis Affected Body Surface Area (BSA) at Week 16
BSA is a measurement of involved skin. The overall BSA affected by psoriasis is estimated based on the palm area of the subject's hand (entire palmar surface or "handprint" including the fingers), which equates to approximately 1% of total body surface area.
Measured: Baseline to Week 16
Percent Change From Baseline in the Psoriasis Area and Severity Index (PASI) Score
The PASI is a measure of psoriatic disease severity taking into account qualitative lesion characteristics (erythema, thickness, and scaling) and degree of skin surface area involvement on defined anatomical regions. The PASI is a validated instrument that has become standard in clinical trials for psoriasis. The PASI scores range from 0 to 72, with higher scores reflecting a greater disease severity.
Measured: Baseline to Week 16
Percentage of Participants Who Achieved a 50% Improvement From Baseline (Response) Reduction in the PASI-50 at Week 16
PASI-50 response is the percentage of participants who achieved at least a 50% reduction (improvement) from baseline in PASI score at Week 16. The improvement in PASI score was used as a measure of efficacy. The PASI was a measure of psoriatic disease severity taking into account qualitative lesion characteristics (erythema, thickness and scaling) and degree of skin surface area involvement on defined anatomical regions. PASI scores range from 0 to 72, with higher scores reflecting greater disease severity. Erythema, thickness, and scaling are scored on a scale of 0 (none) to 4 (very severe) on 4 anatomic regions of the body: head, trunk, upper limbs, and lower limbs. Degree of involvement on each of the 4 anatomic regions is scored on a scale of 0 (no involvement) to 6 (90% to 100% involvement). The PASI score was set to missing if any severity score or degree of involvement is missing.
Measured: Baseline to Week 16
Change From Baseline in Pruritus Visual Analogue Scale 100-mm (VAS) at Week 16
The pruritus visual analog scale (VAS) was used to measure the amount of itching and discomfort a participant experiences. Participant's assessment of pruritus (Itch) asked: On average, how much itch have you had because of your condition in the past week? Higher scores correspond to more severe symptom or disease. The participant places a vertical line on a 100-mm VAS on which the left-hand boundary represents no itch at all and the right-hand boundary represents the worst itch imaginable. The distance from the vertical line to the left-hand boundary is recorded. VAS scores range from 0 to 100 mm, where higher scores correspond to worse pruritis (itch).
Measured: Baseline to Week 16
Change From Baseline in the Dermatology Life Quality Index (DLQI) Total Score at Week 16
Dermatology Life Quality Index (DLQI) was developed as a practical questionnaire for use in a dermatology clinical setting to assess limitations related to the impact of skin disease. The instrument contains 10 items dealing with the participants skin. With the exception of Item Number 7, the participant responds on a four-point scale, ranging from "Very Much" (score 3) to "Not at All" or "Not relevant" (score 0). Item Number 7 is a multi-part item, the first part of which ascertains whether the participant's skin prevented them from working or studying (Yes or No, scores 3 or 0 respectively), and if "No," then the participant is asked how much of a problem the skin has been at work or study over the past week, with response alternatives being "A lot," "A little," or "Not at all" (scores 2, 1, or 0 respectively). The DLQI total score has a possible range from 0 to 30, with 30 corresponding to the worst quality of life, and 0 corresponding to the best.
Measured: Baseline to Week 16
Change From Baseline in Mental Component Summary (MCS) Score of the Medical Outcome Study Short Form 36-item (SF-36) Health Survey Version 2.0 at Week 16
SF-36 is a 36-item general health status instrument often used in clinical trials and health services research. It consists of 8 scales: physical function (PF), role limitations-physical (RP), vitality (VT), general health perceptions (GH), bodily pain (BP), social function (SF), role limitations-emotional (RE), and mental health (MH). Scale scores range from 0 to 100, with higher scores indicating better quality of life (better functioning)
Measured: Baseline to Week 16
Number of Participants Who Achieved an American College of Rheumatology Criteria (ACR) 20% Improvement (ACR 20)
The ACR 20 is defined as a 20% improvement in joint tenderness (78 joint count) and joint swelling scores (76 joint count) compared to baseline plus 20% improvements in 3 of the following 5 assessments (compared to baseline): subject global assessment of disease activity (measured on a 100-mm visual analog scale [VAS]); physician global assessment of disease activity (measured on a 100-mm VAS); subject self-assessment of physical function (Health Assessment Questionnaire - Disability Index [HAQ-DI] score); subject assessment of pain (measured on a 100-mm VAS); and CRP level.
Measured: Baseline to Week 16
Percent Change From Baseline Psoriatic Arthritis Pain Visual Analogue Scale (VAS)
Change from baseline in psoriatic arthritis pain 100-mm VAS; The participant places a vertical line on a 100-mm VAS on which the left-hand boundary represents no pain at all and the right-hand boundary represents the worst possible pain. The distance from the vertical line to the left-hand boundary is recorded.
Measured: Baseline to Week 16
Percent Change From Baseline in Physical Function Assessment Using the Health Assessment Questionnaire Disability Index (HAQ-DI)
Change from baseline in physical function assessment using HAQ-DI; The HAQ-DI is a 20-question, self-administered instrument that measures the subject's functional ability on a 4-level difficulty scale (0-3, with 0 representing normal or no difficulty; and 3 representing inability to perform). Eight categories of functioning are included: dressing, rising, eating, walking, hygiene, reach, grip, and usual activities.
Measured: Baseline to Week 16
Number of Participants With Adverse Events (AE) in the Placebo Controlled Phase
An AE was any noxious, unintended, or untoward medical occurrence, that may appear or worsen in a participant during the course of study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values regardless of etiology. Any worsening (ie, any clinically significant adverse change in the frequency or intensity of a preexisting condition) was considered an AE. A serious AE (SAE) is any untoward adverse event that is fatal, life-threatening, results in persistent or significant disability or incapacity, requires or prolongs existing in-patient hospitalization, is a congenital anomaly or birth defect, or a condition that may jeopardize the patient or may require intervention to prevent one of the outcomes listed above. An AE is a treatment emergent AE if the AE start date is on or after the date of the first dose of study drug and no later than 28 days after the last dose.
Measured: Baseline to Week 16
Number of Participants With Adverse Events (AE) in the During the Apremilast-exposure Period
An AE was any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values regardless of etiology. Any worsening (ie, any clinically significant adverse change in the frequency or intensity of a preexisting condition) was considered an AE. A serious AE (SAE) is any untoward adverse event that is fatal, life-threatening, results in persistent or significant disability or incapacity, requires or prolongs existing in-patient hospitalization, is a congenital anomaly or birth defect, or a condition that may jeopardize the patient or may require intervention to prevent one of the outcomes listed above. An AE is a treatment emergent AE if the AE start date is on or after the date of the first dose of study drug and no later than 28 days after the last dose.
Measured: From the first dose of apremilast (either Week 0 or Week 16 for participants originally randomized to placebo who were re-randomized at Week 16) until 28 days after the last dose of apremilast.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Nov 2013 (estimated)
- Study start9 Jul 2013
- Primary completion20 Nov 2014
- Study completion15 Dec 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for PsoriasisStudies of the same condition, open and under way.
- More trials run by AmgenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 254 participants (actual)
Sponsor and investigators
- Lead sponsor
- Amgen
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- MD, Study director, Amgen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01988103
- Sponsor's protocol ID
- CC-10004-PSOR-011
- Status last verified
- Apr 2020
- First submitted
- 24 May 2013
- Last updated
- 7 May 2020
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- Yes: De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request
Publications
Ohtsuki M, Okubo Y, Komine M, Imafuku S, Day RM, Chen P, Petric R, Maroli A, Nemoto O. Apremilast, an oral phosphodiesterase 4 inhibitor, in the treatment of Japanese patients with moderate to severe plaque psoriasis: Efficacy, safety and tolerability results from a phase 2b randomized controlled trial. J Dermatol. 2017 Aug;44(8):873-884. doi: 10.1111/1346-8138.13829. Epub 2017 Apr 9.
PubMed 28391657Ohtsuki M, Kubo H, Morishima H, Goto R, Zheng R, Nakagawa H. Guselkumab, an anti-interleukin-23 monoclonal antibody, for the treatment of moderate to severe plaque-type psoriasis in Japanese patients: Efficacy and safety results from a phase 3, randomized, double-blind, placebo-controlled study. J Dermatol. 2018 Sep;45(9):1053-1062. doi: 10.1111/1346-8138.14504. Epub 2018 Jun 15.
PubMed 29905383Mease PJ, Hatemi G, Paris M, Cheng S, Maes P, Zhang W, Shi R, Flower A, Picard H, Stein Gold L. Apremilast Long-Term Safety Up to 5 Years from 15 Pooled Randomized, Placebo-Controlled Studies of Psoriasis, Psoriatic Arthritis, and Behcet's Syndrome. Am J Clin Dermatol. 2023 Sep;24(5):809-820. doi: 10.1007/s40257-023-00783-7. Epub 2023 Jun 14.
PubMed 37316690
Study at a glance
From the registry record, last updated by the sponsor on 7 May 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 2B, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Two Doses of Apremilast (CC-10004) In Japanese Subjects With Moderate-To-Severe Plaque-Type Psoriasis
- ClinicalTrials.gov ID
- NCT01988103
- Acronym / sponsor ID
- CC-10004-PSOR-011
- Conditions
- Psoriasis, Psoriatic Arthritis, Psoriasis Arthropatica
- Keywords
- Psoriasis; Psoriatic Arthritis
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 254 participants (actual)
- Lead sponsor
- AmgenIndustry (pharma, biotech, devices)
- Study start
- 9 Jul 2013 (actual)
- Primary completion
- 20 Nov 2014 (actual)
- Study completion
- 15 Dec 2015 (actual)
- First posted
- 20 Nov 2013 (estimated)
- Results
- Posted 20 Mar 2020
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will test the clinical effectiveness and safety of two orally administered doses of apremilast compared to placebo in Japanese patients with moderate-to-severe plaque-type psoriasis.
Detailed description
This is a phase 2b, multicenter, randomized, double-blind, placebo-controlled study of the efficacy and safety of apremilast 20 mg twice a day (BID), apremilast 30 mg BID, and placebo in Japanese participants with moderate to severe plaque psoriasis.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Apremilast 20mg | Experimental | Drug: Apremilast, Drug: PlaceboApremilast 20 mg tablets orally twice a day (BID) |
| Apremilast 30mg | Experimental | Drug: Apremilast, Drug: PlaceboApremilast 30 mg tablets orally BID |
| Placebo | Placebo comparator | Drug: PlaceboIdentically-appearing placebo tablets BID for 16 weeks followed by participants being re-randomized in a blinded fasion to apremilast 20 mg or 30mg tablets BID for 52 weeks |
Who may qualify
- Ages
- 20 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Male or female Japanese participants greater than or equal to 20 years of age.
- Diagnosis of chronic, stable plaque psoriasis for at least 6 months prior to screening as defined by: Psoriasis Area Severity Index (PASI) score ≥ 12 and BSA ≥ 10%.
- Psoriasis which is considered inappropriate for topical therapy (based on severity of disease and extent of affected area) or has not been adequately controlled or treated by topical therapy in spite of at least 4 weeks of prior therapy with at least one topical medication for psoriasis or per label.
- In otherwise good health based on medical history, physical examination, 12-lead electrocardiogram (ECG), serum chemistry, hematology, immunology, and urinalysis.
Key exclusion criteria (15 listed)
- Other than psoriasis, history of any clinically significant and uncontrolled systemic diseases; any condition, including the presence of laboratory abnormalities, which would place the participant at unacceptable risk or confound the ability to interpret the data in the study.
- Prior medical history of suicide attempt or major psychiatric illness requiring hospitalization within the last 3 years
- Pregnant or breastfeeding.
- History of or ongoing chronic or recurrent infectious disease.
- Active tuberculosis (TB) or a history of incompletely treated TB.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ApremilastAlso: CC-10004, Otzela20 mg tablet BID for 68 weeks | Drug | Apremilast 20mg |
| ApremilastAlso: CC-10004, Otzela20 mg tablet BID for 68 weeks | Drug | Apremilast 30mg |
| PlaceboPlacebo tablet BID for 16 weeks | Drug | Apremilast 20mg, Apremilast 30mg, Placebo |
Primary outcome
Percentage of Participants Who Achieved a 75% Improvement (Response) From Baseline in the Psoriasis Area and Severity Index (PASI-75) at Week 16
Time frame: Baseline to Week 16
PASI-75 response is the percentage of participants who achieved at least a 75% reduction (improvement) from baseline in PASI score at Week 16. The improvement in PASI score was used as a measure of efficacy. The PASI was a measure of psoriatic disease severity taking into account qualitative lesion characteristics (erythema, thickness and scaling) and degree of skin surface area involvement on defined anatomical regions. PASI scores range from 0 to 72, with higher scores reflecting greater disease severity. Erythema, thickness, and scaling are scored on a scale of 0 (none) to 4 (very severe) on 4 anatomic regions of the body: head, trunk, upper limbs, and lower limbs. Degree of involvement on each of the 4 anatomic regions is scored on a scale of 0 (no involvement) to 6 (90% to 100% involvement). The PASI score was set to missing if any severity score or degree of involvement was missing.
12 secondary outcomes
Percentage of Participants Who Achieved a Static Physician's Global Assessment (sPGA) Score of Clear (0) or Almost Clear (1) With at Least 2 Point Reduction From Baseline to Week 16
Time frame: Baseline to Week 16
Percent Change From Baseline in the Psoriasis Affected Body Surface Area (BSA) at Week 16
Time frame: Baseline to Week 16
Percent Change From Baseline in the Psoriasis Area and Severity Index (PASI) Score
Time frame: Baseline to Week 16
Percentage of Participants Who Achieved a 50% Improvement From Baseline (Response) Reduction in the PASI-50 at Week 16
Time frame: Baseline to Week 16
Change From Baseline in Pruritus Visual Analogue Scale 100-mm (VAS) at Week 16
Time frame: Baseline to Week 16
Change From Baseline in the Dermatology Life Quality Index (DLQI) Total Score at Week 16
Time frame: Baseline to Week 16
Change From Baseline in Mental Component Summary (MCS) Score of the Medical Outcome Study Short Form 36-item (SF-36) Health Survey Version 2.0 at Week 16
Time frame: Baseline to Week 16
Number of Participants Who Achieved an American College of Rheumatology Criteria (ACR) 20% Improvement (ACR 20)
Time frame: Baseline to Week 16
Percent Change From Baseline Psoriatic Arthritis Pain Visual Analogue Scale (VAS)
Time frame: Baseline to Week 16
Percent Change From Baseline in Physical Function Assessment Using the Health Assessment Questionnaire Disability Index (HAQ-DI)
Time frame: Baseline to Week 16
Number of Participants With Adverse Events (AE) in the Placebo Controlled Phase
Time frame: Baseline to Week 16
Number of Participants With Adverse Events (AE) in the During the Apremilast-exposure Period
Time frame: From the first dose of apremilast (either Week 0 or Week 16 for participants originally randomized to placebo who were re-randomized at Week 16) until 28 days after the last dose of apremilast.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 May 2020.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Background: PubMed 28391657Ohtsuki M, Okubo Y, Komine M, Imafuku S, Day RM, Chen P, Petric R, Maroli A, Nemoto O. Apremilast, an oral phosphodiesterase 4 inhibitor, in the treatment of Japanese patients with moderate to severe plaque psoriasis: Efficacy, safety and tolerability results from a phase 2b randomized controlled trial. J Dermatol. 2017 Aug;44(8):873-884. doi: 10.1111/1346-8138.13829. Epub 2017 Apr 9.
- Background: PubMed 29905383Ohtsuki M, Kubo H, Morishima H, Goto R, Zheng R, Nakagawa H. Guselkumab, an anti-interleukin-23 monoclonal antibody, for the treatment of moderate to severe plaque-type psoriasis in Japanese patients: Efficacy and safety results from a phase 3, randomized, double-blind, placebo-controlled study. J Dermatol. 2018 Sep;45(9):1053-1062. doi: 10.1111/1346-8138.14504. Epub 2018 Jun 15.
- Derived from this study: PubMed 37316690Mease PJ, Hatemi G, Paris M, Cheng S, Maes P, Zhang W, Shi R, Flower A, Picard H, Stein Gold L. Apremilast Long-Term Safety Up to 5 Years from 15 Pooled Randomized, Placebo-Controlled Studies of Psoriasis, Psoriatic Arthritis, and Behcet's Syndrome. Am J Clin Dermatol. 2023 Sep;24(5):809-820. doi: 10.1007/s40257-023-00783-7. Epub 2023 Jun 14.
- Individual participant dataSharing planned: Yes. De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
MD study director
Amgen
56 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Apremilast in people with Psoriasis and Psoriatic Arthritis, run by Amgen at 56 sites in Japan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 7 May 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 56 sites in Japan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 20 Mar 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Participants Who Achieved a 75% Improvement (Response) From Baseline in the Psoriasis Area and Severity Index (PASI-75) at Week 16 (time frame: Baseline to Week 16). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01988103, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 May 2020.